3D model (JSmol)
CompTox Dashboard (EPA)
|Molar mass||120.19 g/mol|
|Melting point||−43.78 °C (−46.80 °F; 229.37 K)|
|Boiling point||169 to 171 °C (336 to 340 °F; 442 to 444 K)|
|Safety data sheet||Sigma-Aldrich MSDS|
|Harmful (Xn); Dangerous for the environment (N)|
|Flash point||44.4 °C (111.9 °F; 317.5 K)|
|US health exposure limits (NIOSH):|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
1,2,4-Trimethylbenzene, also known as pseudocumene, is an organic compound with the chemical formula C6H3(CH3)3. Classified as an aromatic hydrocarbon, it is a flammable colorless liquid with a strong odor. It is nearly insoluble in water but soluble in organic solvents. It occurs naturally in coal tar and petroleum (about 3%).
Industrially, it is isolated from the C9 aromatic hydrocarbon fraction during petroleum distillation. Approximately 40% of this fraction is 1,2,4-trimethylbenzene. It is also generated by methylation of toluene and xylenes and the disproportionation of xylene over aluminosilicate catalysts.
Pseudocumene is a precursor to mellitic anhydride, from which high performance polymers are made. It is also used as a sterilizing agent and in the making of dyes, perfumes and resins. Another use is as a gasoline additive.
- Merck Index, 11th Edition, 7929
- NIOSH Pocket Guide to Chemical Hazards. "#0638". National Institute for Occupational Safety and Health (NIOSH).
- Karl Griesbaum, Arno Behr, Dieter Biedenkapp, Heinz-Werner Voges, Dorothea Garbe, Christian Paetz, Gerd Collin, Dieter Mayer, Hartmut Höke "Hydrocarbons" in Ullmann's Encyclopedia of Industrial Chemistry 2002 Wiley-VCH, Weinheim. doi:10.1002/14356007.a13_227
- "Chemical Summary for 1,2,4-Trimethylbenzene" (text). United States Environmental Protection Agency. 1994-08-01. Retrieved 2008-01-28.
- Mufson, S.; et al. (November 1, 2015). "Liquid scintillator production for the NOvA experiment". Nuclear Instruments and Methods A. 799: 1. arXiv:1504.04035. Bibcode:2015NIMPA.799....1M. doi:10.1016/j.nima.2015.07.026. Retrieved 2016-06-15.